- ¥600 - 2280
- 信裕生物
- 78-5000pg/ml
- XY-EH0777
- 进口/国产
- 2025年09月05日
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- 详细信息
- 文献和实验
- 技术资料
- 样本：
血清、血浆或其它相关生物液体中天然和重组CYP3A4蛋白
- 库存：
30
- 标记物：
血清/血桨/组织等
- 适应物种：
人
- 应用：
用于科研使用
- 检测方法：
酶联免疫吸附测定法
- 检测范围：
78-5000pg/ml
- 供应商：
上海信裕生物科技有限公司
- 规格：
48T/96T
| Product name | Human CYP3A4(Cytochrome P450 3A4) ELISA Kit |
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| Catalogue No. | XY-EH0777 | ||||||||||||||||||||
| Alias | CYP3A4 (Cytochrome P450 3A4) ELISA Kit, CYP3A3 CYPIIIA3 ELISA Kit, CYPIIIA4 ELISA Kit, Nifedipine ELISA Kit, 8-cineole 2-exo-monooxygenase ELISA Kit, Albendazole monooxygenase ELISA Kit, Albendazole sulfoxidase ELISA Kit, Cytochrome P450 3A3 ELISA Kit, Cytochrome P450 HLp ELISA Kit, Cytochrome P450 NF-25 ELISA Kit, Cytochrome P450-PCN1 ELISA Kit |
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| Detection method | Sandwich ELISA, Double Antibody |
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| Size | 96T |
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| Range | 78-5000pg/ml |
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| Sensitivity | < 46.9pg/ml |
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| Standard curve |  |
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| Storage | 4 ℃ for 6 months |
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| Recovery | Matrices listed below were spiked with certain level of CYP3A4 and the recovery rates were calculated by comparing the measured value to the expected amount of CYP3A4 in samples.
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| Linearity | The linearity of the kit was assayed by testing samples spiked with appropriate concentration of CYP3A4 and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.
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| CV(%) | Intra-Assay: CV<8% |
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| Note | For Research Use Only |
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文献和实验Warnings And Limitations This product is for research use only. Not intended for any animal or human therapeutic or diagnostic use unless otherwise stated. Follow appropriate laboratory guidelines. This product contains 0.02% sodium azide
RAT/MOUSE GROWTH HORMONE ELISA KIT
实验原理 This assay is a Sandwich ELISA based, sequentially, on: 1) capture of rat or mouse Growth Hormone molecules from samples to the wells of a microtiter plate coated by a pre-titered amount of anti-Growth Hormone
Evaluation of Time-Dependent CYP3A4 Inhibition Using Human Hepatocytes
prediction algorithms have been developed, the accuracy has still improved little. This suggests alternate methods to collect input data may improve prediction robustness. Historically, human liver microsomes have been used to generate inhibition kinetic data
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